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Founded in 2012, IMed Consultancy offers a wide range of regulatory and compliance services to the medical technology industry, supporting medical device and IVD manufacturers through all stages of the product lifecycle from: designing an initial regulatory strategy, authoring technical documentation and clinical literature reviews right through to post market surveillance activities, as well as all aspects of writing, implementing and maintaining a Quality Management System. IMed Consultancy’s team of highly skilled and experienced medical regulatory professionals offer an outstanding yet flexible service covering Regulatory Affairs, UKRP and EUAR services, PRRC and QA in medical devices, including Class III, active & implantables, companion diagnostics, Software as a medical Device (SaMD) and IVDs. With extensive hands-on problem-solving expertise, IMed’s remit is truly global, ensuring that client devices are successfully launched and maintained in total compliance in the UK, EU, US and internationally.
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